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Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland. (2025)

First Author: Watson-Fargie T

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2025.105343

PubMed Identifier: 40157166

Publication URI: http://europepmc.org/abstract/MED/40157166

Type: Journal Article/Review

Volume: 49

Parent Publication: Neuromuscular disorders : NMD

ISSN: 0960-8966